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SYNTHES DISTRACTION OSTEOGENESIS SYSTEM, MR CONDITIONAL WITH EXPANDED INDICATIONS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092190
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2010
Days to Decision
294 days
Submission Type
Summary

SYNTHES DISTRACTION OSTEOGENESIS SYSTEM, MR CONDITIONAL WITH EXPANDED INDICATIONS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092190
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2010
Days to Decision
294 days
Submission Type
Summary